Splenic Lymphatic Malformation With Papillary Endothelial Proliferation: A Rare Histologic Variant or a Unique Entity?

JC Slack, J Putra, MJ Callahan, AJ Church… - The American Journal …, 2023 - journals.lww.com
Lymphatic malformations (LMs) are congenital anomalies of the lymphatic system due to
abnormalities that occur during the development of the lymphovascular system. Also known …

Splenic hemangioma as a potential pitfall on PSMA-targeted 18F-DCFPyL PET/CT

G Chaussé, J Laufer, G Abikhzer… - Clinical Nuclear …, 2019 - journals.lww.com
A 69-year-old man with biochemical recurrence after radical prostatectomy underwent 6
months of androgen deprivation therapy. Upon discontinuation of androgen deprivation …

Splenic lymphangiomas as a common indication for splenectomy: a case series with literature review

B Efared, ABA Bako, H Younssa, I Boubacar… - BMC surgery, 2022 - Springer
Background Splenic lymphangiomas (SL) are very rare benign cystic lesions found in
pediatric population. Their occurrence in adults is exceptional. Splenectomy is the common …

MARKED ACANTHOCYTOSIS ASSOCIATED WITH KLIPPLE-TRENAUNAY SYNDROME.

SM Ali, N Raza, E Aftab… - Journal of Ayub …, 2023 - search.ebscohost.com
Klipple-Trenaunay syndrome (KTS) is an extremely rare congenital vascular disorder with
poorly defined incidence and prevalence. We report a case of a patient who presented after …

Klippel-Trenaunay Syndrome: A Review Article.

A Mungnirandr - Journal of the Medical Association of …, 2020 - search.ebscohost.com
Klippel-Trenaunay syndrome is a vascular malformation associated with limb overgrowth
(1). The name of the disease came from two French men: Maurice Klippel and Paul …

[PDF][PDF] Retroperitoneal Mass-Lesion with Calcificaction; Cystic Lymphangioma; Case Report

A Moradi, A Hajian, A Davoodabadi… - Journal of Surgery, 2019 - researchgate.net
Lymphangioma in retroperitoneum is a rare mass-like lesion which presented
histopatholigically with single or multi-cystic type and/or cavernous type; and clinically is …

Klippel− Trenaunay Syndrome

D Liu - Handbook of Tumor Syndromes, 2020 - taylorfrancis.com
Klippel–Trenaunay syndrome (KTS) is a rare congenital disorder that typically displays
characteristic features: port-wine stain, abnormal overgrowth of soft tissues and bones, and …

[引用][C] Marked acanthocytosis in the setting of Klippel‐Trenaunay syndrome: A case report

H Cruz, AM Ferreira, E Costa, J Barbot… - … Journal of Laboratory …, 2019 - Wiley Online Library